Key result
Aspirin use is not linked to the risk of developing MAFLD.
Why the study?
This study investigated the association between aspirin use and metabolic dysfunction-associated fatty liver disease.
Does aspirin use prevent metabolic dysfunction-associated fatty liver disease in a general population cohort?
Observational (n=3,922)
Yes
Does aspirin use prevent metabolic dysfunction-associated fatty liver disease in a general population cohort?
Odds Ratio: 0.97 (95% CI 0.82–1.15)
p-value: p=0.718
In a large propensity-matched cohort from the UK Biobank, aspirin use was not significantly associated with a reduced risk of metabolic dysfunction-associated fatty liver disease, though exploratory analyses suggested a potential benefit in obese individuals.
No MAFLD prevention signal with aspirin overall; hypothesis-generating for obese subgroup benefit pending prospective trials.
This study investigated the association between aspirin use and metabolic dysfunction-associated fatty liver disease (MAFLD). Based on data from the UK Biobank (UKB), this study included a variety of covariates such as age, gender, BMI, lifestyle factors, metabolic indicators and liver function indicators, and assessed the association between aspirin use and MAFLD after balancing the baseline differences by the propensity score matching (PSM) method, and explored the influencing factors by stratified analyses and interaction tests. During a median follow-up period of 9.41 years, among 3,922 participants, aspirin use was not significantly associated with MAFLD after adjusting for a variety of metabolic confounders (OR = 0.97, 95% CI: 0.82–1.15), a finding that was consistent across sensitivity analyses. When BMI was modeled categorically, a significant association was observed only among participants with obesity (BMI ≥ 30 kg/m²; OR 0.69, 95% CI 0.52–0.92), whereas no associations were found in normal-weight or overweight groups. An exploratory interaction was observed between aspirin use and stroke history (aspirin × stroke, OR for interaction = 0.07, 95% CI: 0.008–0.646, P = 0.019). In this observational study, aspirin use was not significantly associated with MAFLD. Exploratory analyses suggested possible heterogeneity according to BMI and stroke history; however, these findings should be considered hypothesis-generating because of multiple comparisons and the small number of participants with a history of stroke. Overall, aspirin use was not significantly associated with MAFLD.
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Song et al. (2026) conducted an observational in Metabolic dysfunction-associated fatty liver disease (MAFLD) (n=3,922). Aspirin use vs. Non-aspirin users was evaluated on Risk of developing MAFLD (OR 0.97, 95% CI 0.82-1.15, p=0.718). Aspirin use was not significantly associated with the risk of metabolic dysfunction-associated fatty liver disease (OR 0.97) after adjusting for metabolic confounders.
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